rs1059455

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs1059455(C;G)

Make rs1059455(G;G)

Reference

GRCh38 38.1/141

Chromosome

6

Position

29942939

Gene

HLA-A

is a	snp
is	mentioned by
dbSNP	rs1059455
dbSNP (classic)	rs1059455
ClinGen	rs1059455
ebi	rs1059455
HLI	rs1059455
Exac	rs1059455
Gnomad	rs1059455
Varsome	rs1059455
LitVar	rs1059455
Map	rs1059455
PheGenI	rs1059455
Biobank	rs1059455
1000 genomes	rs1059455
hgdp	rs1059455
ensembl	rs1059455
geneview	rs1059455
scholar	rs1059455
google	rs1059455
pharmgkb	rs1059455
gwascentral	rs1059455
openSNP	rs1059455
23andMe	rs1059455
SNPshot	rs1059455
SNPdbe	rs1059455
MSV3d	rs1059455
GWAS Ctlg	rs1059455

Max Magnitude

0

ClinVar
Risk	rs1059455(A;A) rs1059455(G;G)
Alt	rs1059455(A;A) rs1059455(G;G)
Reference	Rs1059455(C;C)
Significance	Histocompatibility
Disease
Variation	info
Gene	HLA-A
CLNDBN
Reversed	0
HGVS	NC_000006.11:g.29910716C>A; NC_000006.11:g.29910716C>G
CLNSRC
CLNACC